Vascular NADPH oxidases as drug targets for novel antioxidant strategies

被引:171
作者
Guzik, Tomasz J. [1 ]
Harrison, David G.
机构
[1] Emory Univ, Sch Med, Div Cardiol, Atlanta, GA 30322 USA
[2] Jagiellonian Univ, Sch Med, Dept Pharmacol, PL-31101 Krakow, Poland
[3] Jagiellonian Univ, Sch Med, Dept Med, PL-31101 Krakow, Poland
关键词
D O I
10.1016/j.drudis.2006.04.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Reactive oxygen species (ROS) play important roles in the pathogenesis of cardiovascular disease. Surprisingly, large clinical trials have shown that ROS scavenging by antioxidant vitamins is ineffective or harmful. Therefore, prevention of ROS formation, by targeting specific sources of superoxide anion and other ROS, might prove beneficial. Potential targets include the NADPH oxidases (Nox enzymes), xanthine oxidase, endothelial nitric oxide synthase and mitochondrial oxidases. Nox enzymes play a central role because they can regulate other enzymatic sources of ROS. Statins, angiotensin-converting enzyme inhibitors and angiotensin receptor antagonists block upstream signaling of Nox activation, which contributes to their clinical effectiveness. Here, we discuss novel possibilities where drugs that directly inhibit Nox activation could successfully inhibit oxidative stress.
引用
收藏
页码:524 / 533
页数:10
相关论文
共 82 条
[51]   Redox mechanisms in blood vessels [J].
Mueller, CFH ;
Laude, K ;
McNally, JS ;
Harrison, DG .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (02) :274-278
[52]   RELEASE OF INTACT ENDOTHELIUM-DERIVED RELAXING FACTOR DEPENDS ON ENDOTHELIAL SUPEROXIDE-DISMUTASE ACTIVITY [J].
MUGGE, A ;
ELWELL, JH ;
PETERSON, TE ;
HARRISON, DG .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (02) :C219-C225
[53]   Multiple role of reactive oxygen species in the arterial wall [J].
Napoli, C ;
de Nigris, F ;
Palinski, W .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2001, 82 (04) :674-682
[54]   MODULAR STRUCTURE OF NEURONAL NITRIC-OXIDE SYNTHASE - LOCALIZATION OF THE ARGININE BINDING-SITE AND MODULATION BY PTERIN [J].
NISHIMURA, JS ;
MARTASEK, P ;
MCMILLAN, K ;
SALERNO, JC ;
LIU, Q ;
GROSS, SS ;
MASTERS, BSS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 210 (02) :288-294
[55]   HYPERCHOLESTEROLEMIA INCREASES ENDOTHELIAL SUPEROXIDE ANION PRODUCTION [J].
OHARA, Y ;
PETERSON, TE ;
HARRISON, DG .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (06) :2546-2551
[56]   DIETARY CORRECTION OF HYPERCHOLESTEROLEMIA IN THE RABBIT NORMALIZES ENDOTHELIAL SUPEROXIDE ANION PRODUCTION [J].
OHARA, Y ;
PETERSON, TE ;
SAYEGH, HS ;
SUBRAMANIAN, RR ;
WILCOX, JN ;
HARRISON, DG .
CIRCULATION, 1995, 92 (04) :898-903
[57]   Chronic oral supplementation with sepiapterin prevents endothelial dysfunction and oxidative stress in small mesenteric arteries from diabetic (db/db) mice [J].
Pannirselvam, M ;
Simon, V ;
Verma, S ;
Anderson, T ;
Triggle, CR .
BRITISH JOURNAL OF PHARMACOLOGY, 2003, 140 (04) :701-706
[58]   Angiotensin II-mediated hypertension in the rat increases vascular superoxide production via membrane NADH/NADPH oxidase activation - Contribution to alterations of vasomotor tone [J].
Rajagopalan, S ;
Kurz, S ;
Munzel, T ;
Tarpey, M ;
Freeman, BA ;
Griendling, KK ;
Harrison, DG .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (08) :1916-1923
[59]   Reversing endothelial dysfunction with ACE inhibitors - A new trend? [J].
Rajagopalan, S ;
Harrison, DG .
CIRCULATION, 1996, 94 (03) :240-243
[60]   Novel competitive inhibitor of NAD(P)H oxidase assembly attenuates vascular O2- and systolic blood pressure in mice [J].
Rey, FE ;
Cifuentes, ME ;
Kiarash, A ;
Quinn, MT ;
Pagano, PJ .
CIRCULATION RESEARCH, 2001, 89 (05) :408-414